HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253130Generated: November 3, 2026
Vinylidene chloride → 1,1-Dichloro-3,3,4-trimethylpent-1-ene
https://huagongshe.com/reaction/1253130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vinylidene chloride | HCID 6366 | — |
| Reactant | 2-Chloro-2,3-dimethylbutane | HCID 136383 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,1-Dichloro-3,3,4-trimethylpent-1-ene | HCID 13295224 | 65% |
Reaction Steps
20 g of anhydrous, powdered aluminum chloride are added in portions to 2,040 g (21 mols) of vinylidene chloride at -10° C., in a dry apparatus equipped with a drying tube. 837 g (7 mols) of 2-chloro-2,3-dimethylbutane are then added dropwise in the temperature range from 0° to 10° C. The mixture is allowed to warm up to 20° C., and further aluminum chloride portions (a maximum of 20 g) are added, while cooling, until the reaction is no longer exothermic. The mixture is stirred for a further 4 hours at room temperature, the catalyst is deactivated by dropwise addition of 70 ml of acetic acid, and the mixture is filtered over sodium sulphate. The volatile constituents are separated from the sparingly volatile constituents by continuous-feed distillation under 1 mbar. The distillate is fractionated in a column. 824 g (65% of theory) of 1,1-dichloro-3,3,4-trimethyl-pent-1-ene of boiling point 60°-75° C./20 mbar are obtained. ##STR19##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04747869 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-863c4439291d4ced802e61be3e1e32d8 |
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| Source note | uspto-grants-1988_05 |
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